Boronic acid derivatives
Aobchem 4-Acetyl-3-fluorophenylboronic acid pinacol ester | ≥97% | CAS 1351499-39-2 | C14H18BFO3 | 5g
4-Acetyl-3-fluorophenylboronic acid pinacol ester | ≥97% | CAS 1351499-39-2 | C14H18BFO3 | 5g
Aobchem 2-Bromo-6-fluorophenylboronic acid pinacol ester | ≥95% | CAS 1595078-06-0 | C12H15BBrFO2 | 500mg
2-Bromo-6-fluorophenylboronic acid pinacol ester | ≥95% | CAS 1595078-06-0 | C12H15BBrFO2 | 500mg
Aobchem 4-Methoxy-2-nitrophenylboronic acid pinacol ester | ≥97% | CAS 1073353-81-7 | C13H18BNO5 | 5g
4-Methoxy-2-nitrophenylboronic acid pinacol ester | ≥97% | CAS 1073353-81-7 | C13H18BNO5 | 5g
Aobchem 2 4-Dichlorophenylboronic acid pinacol ester | ≥97% | CAS 68716-50-7 | C12H15BCl2O2 | 25g
2 4-Dichlorophenylboronic acid pinacol ester | ≥97% | CAS 68716-50-7 | C12H15BCl2O2 | 25g
Aobchem 3-Ethoxy-2-fluorophenylboronic acid | ≥97% | CAS 855230-61-4 | C8H10BFO3 | 5g
3-Ethoxy-2-fluorophenylboronic acid | ≥97% | CAS 855230-61-4 | C8H10BFO3 | 5g
Aobchem 4-Hexyloxyphenylboronic acid | ≥95% | CAS 121219-08-7 | C12H19BO3 | 10g
4-Hexyloxyphenylboronic acid | ≥95% | CAS 121219-08-7 | C12H19BO3 | 10g
![Frontier Specialty Chemicals 5g, 1-Cyclohexenylboronic acid pinacol ester, 98%, [141091-37-4], C10330 208.105 C12H21BO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Frontier Specialty Chemicals 5g, 1-Cyclohexenylboronic acid pinacol ester, 98%, [141091-37-4], C10330 208.105 C12H21BO2
Compound: 1-Cyclohexenylboronic acid pinacol ester
CAS#: 141091-37-4
MDL#: MFCD05663845
Background: A cyclic vinylboronic ester widely used as a coupling partner in Suzuki-Miyaura cross-coupling reactions to introduce a cyclohexenyl group into target molecules. It is a common building block in pharmaceutical and natural product synthesis.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, 1-Cyclohexenylboronic acid pinacol ester, 98%, [141091-37-4], C10330 208.105 C12H21BO2
Compound: 1-Cyclohexenylboronic acid pinacol ester
CAS#: 141091-37-4
MDL#: MFCD05663845
Background: A cyclic vinylboronic ester widely used as a coupling partner in Suzuki-Miyaura cross-coupling reactions to introduce a cyclohexenyl group into target molecules. It is a common building block in pharmaceutical and natural product synthesis.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 25g, 1-Pentenylboronic acid, 98%, [104376-24-1], P11073 113.951 C5H11BO2
Compound: 1-Pentenylboronic acid
CAS#: 104376-24-1
MDL#: not listed
Background: A terminal alkenylboronic acid used as a Suzuki-Miyaura coupling partner in organic synthesis. It provides a convenient means to introduce a pentenyl group into pharmaceutical and agrochemical building blocks.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, Allylboronic acid pinacol ester, 97%, [72824-04-5], A1648 168.05 C9H17BO2
Compound: Allylboronic acid pinacol ester
CAS#: 72824-04-5
MDL#: MFCD00013347
Background: Allylboronic acid pinacol ester is a synthetic specialty chemical useful in the synthesis of pharmaceuticals and specialty organic chemicals. It is commonly used as an allylating reagent in organic synthesis and in transition metal-catalyzed coupling reactions.
Storage: Store at 2-8°C, under dry conditions.
Frontier Specialty Chemicals 25g, Allylboronic acid pinacol ester, 97%, [72824-04-5], A1648 168.05 C9H17BO2
Compound: Allylboronic acid pinacol ester
CAS#: 72824-04-5
MDL#: MFCD00013347
Background: Allylboronic acid pinacol ester is a synthetic specialty chemical useful in the synthesis of pharmaceuticals and specialty organic chemicals. It is commonly used as an allylating reagent in organic synthesis and in transition metal-catalyzed coupling reactions.
Storage: Store at 2-8°C, under dry conditions.
Frontier Specialty Chemicals 5g, 1-Boc-pyrrole-2-boronic acid, 98%, [135884-31-0], B5969 211.02 C9H14BNO4
Compound: 1-Boc-pyrrole-2-boronic acid
CAS#: 135884-31-0
MDL#: MFCD01318939
Background: 1-Boc-pyrrole-2-boronic acid is a protected heteroaryl boronic acid used as a coupling partner in Suzuki-Miyaura cross-coupling reactions. The Boc protecting group allows selective deprotection and further functionalization of the pyrrole ring, making it useful in pharmaceutical synthesis. It has also been applied in the development of sensors for detecting sugars and other biomolecules.
Frontier Specialty Chemicals 5g, 3-(N-Boc-aminomethyl)phenylboronic acid, 98%, [199609-62-6], B9487 251.09 C12H18BNO4
Compound: 3-(N-Boc-aminomethyl)phenylboronic acid
CAS#: 199609-62-6
MDL#: MFCD06246052
Background: A Boc-protected aminomethyl phenylboronic acid used as a building block in Suzuki-Miyaura coupling chemistry. The protected amine allows for later deprotection and further functionalization, and this compound has been applied in the development of drug candidates for cancer and diabetes research.
Storage: Store at 2-8°C, under dry conditions.
Frontier Specialty Chemicals 1g, 3-(N-Boc-aminomethyl)phenylboronic acid, 98%, [199609-62-6], B9487 251.09 C12H18BNO4
Compound: 3-(N-Boc-aminomethyl)phenylboronic acid
CAS#: 199609-62-6
MDL#: MFCD06246052
Background: A Boc-protected aminomethyl phenylboronic acid used as a building block in Suzuki-Miyaura coupling chemistry. The protected amine allows for later deprotection and further functionalization, and this compound has been applied in the development of drug candidates for cancer and diabetes research.
Storage: Store at 2-8°C, under dry conditions.
Frontier Specialty Chemicals 1g, 4-(N-Methylaminocarbonyl)phenylboronic acid, 98%, [121177-82-0], M10870 178.981 C8H10BNO3
Compound: 4-(N-Methylaminocarbonyl)phenylboronic acid
CAS#: 121177-82-0
MDL#: not listed
Background: A secondary amide-substituted phenylboronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical research. The amide N-H offers a site for hydrogen bonding, useful for tuning the physicochemical properties of downstream coupled products.
Storage: Store at room temperature, under dry conditions.